MEG9 - maternally expressed 9 Gene

Also Known as LINC00584

Species: Homo sapiens

Gene Type: ncRNA
Gene ID: 100507257

About MEG9

This gene has 8 transcripts (splice variants). Biased expression in placenta (RPKM 10.0), adrenal (RPKM 8.9) and 7 other tissues.

Related Diseases

Diseases Alias
Kagami-Ogata Syndrome

  • Paternal Uniparental Disomy Of Chromosome 14

  • Uniparental Disomy, Paternal, Chromosome 14

  • Kos

  • Mca Due To 14q32.2 Maternally Expressed Gene Defect

  • Paternal Uniparental Disomy 14

  • Kagami-Ogata Syndrome Due To Maternal 14q32.2 Microdeletion

  • Maternal Del(14)(Q32.2)

  • Maternal Monosomy 14q32.2

  • Kagami-Ogata Syndrome Due To Maternal 14q32.2 Hypermethylation

  • Kagami-Ogata Syndrome Due To Paternal Uniparental Disomy Of Chromosome 14

  • Upd(14)Pat
Astigmatism
Temple Syndrome

  • Uniparental Disomy, Maternal, Chromosome 14

  • Temple Syndrome Due To Paternal 14q32.2 Microdeletion

  • Paternal Del(14)(Q32.2)

  • Temple Syndrome Due To Paternal 14q32.2 Hypomethylation

  • Temple Syndrome Due To Maternal Uniparental Disomy Of Chromosome 14

  • Upd(14)Mat
Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-P3927 [MePhe8,Sar9] Substance P / Unkown